CA2471485C - Process for preparing 2-(substituted phenyl) - 2 - hydroxy-ethyl carbamates - Google Patents
Process for preparing 2-(substituted phenyl) - 2 - hydroxy-ethyl carbamates Download PDFInfo
- Publication number
- CA2471485C CA2471485C CA2471485A CA2471485A CA2471485C CA 2471485 C CA2471485 C CA 2471485C CA 2471485 A CA2471485 A CA 2471485A CA 2471485 A CA2471485 A CA 2471485A CA 2471485 C CA2471485 C CA 2471485C
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- formula
- ethers
- compound
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- ester
- Prior art date
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- -1 2-(substituted phenyl) - 2 - hydroxy-ethyl carbamates Chemical class 0.000 title claims abstract description 25
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 13
- 238000000034 method Methods 0.000 claims abstract description 64
- 230000008569 process Effects 0.000 claims abstract description 46
- 150000001875 compounds Chemical class 0.000 claims description 67
- 150000002148 esters Chemical class 0.000 claims description 21
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
- QBYIENPQHBMVBV-HFEGYEGKSA-N (2R)-2-hydroxy-2-phenylacetic acid Chemical class O[C@@H](C(O)=O)c1ccccc1.O[C@@H](C(O)=O)c1ccccc1 QBYIENPQHBMVBV-HFEGYEGKSA-N 0.000 claims description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 10
- 125000006239 protecting group Chemical group 0.000 claims description 10
- 239000003638 chemical reducing agent Substances 0.000 claims description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
- 229910052987 metal hydride Inorganic materials 0.000 claims description 8
- 150000004681 metal hydrides Chemical group 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 7
- 125000001424 substituent group Chemical group 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 150000001412 amines Chemical class 0.000 claims description 5
- 150000001728 carbonyl compounds Chemical class 0.000 claims description 5
- 239000003153 chemical reaction reagent Substances 0.000 claims description 5
- 125000005843 halogen group Chemical group 0.000 claims description 5
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- IWYDHOAUDWTVEP-UHFFFAOYSA-N R-2-phenyl-2-hydroxyacetic acid Natural products OC(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-N 0.000 claims description 4
- 125000006241 alcohol protecting group Chemical group 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 229960002510 mandelic acid Drugs 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 238000005886 esterification reaction Methods 0.000 claims description 3
- PPJVXZVTPWQOQS-UHFFFAOYSA-N 1-ethoxy-1-(1-ethoxyethoxy)ethane Chemical class CCOC(C)OC(C)OCC PPJVXZVTPWQOQS-UHFFFAOYSA-N 0.000 claims description 2
- YFEXZJKJPFNYKB-UHFFFAOYSA-N 2-(oxolan-2-yloxy)oxolane Chemical class C1CCOC1OC1OCCC1 YFEXZJKJPFNYKB-UHFFFAOYSA-N 0.000 claims description 2
- JMTBNBFBHBCERV-UHFFFAOYSA-N 2-(thiolan-2-yloxy)thiolane Chemical class C1CCSC1OC1SCCC1 JMTBNBFBHBCERV-UHFFFAOYSA-N 0.000 claims description 2
- ZQVMXWDQXLWKLE-UHFFFAOYSA-N 4-methoxy-2-(4-methoxyoxan-2-yl)oxyoxane Chemical class C1C(OC)CCOC1OC1OCCC(OC)C1 ZQVMXWDQXLWKLE-UHFFFAOYSA-N 0.000 claims description 2
- ZXTCTDQZUWWAEY-UHFFFAOYSA-N 4-methoxy-2-(4-methoxythian-2-yl)oxythiane Chemical class C1C(OC)CCSC1OC1SCCC(OC)C1 ZXTCTDQZUWWAEY-UHFFFAOYSA-N 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical class C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 claims description 2
- NSPJNIDYTSSIIY-UHFFFAOYSA-N methoxy(methoxymethoxy)methane Chemical group COCOCOC NSPJNIDYTSSIIY-UHFFFAOYSA-N 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 3
- 230000032050 esterification Effects 0.000 claims 2
- DTCYSRAEJHGSNY-UHFFFAOYSA-N 2-methoxy-2-(2-methoxypropan-2-yloxy)propane Chemical class COC(C)(C)OC(C)(C)OC DTCYSRAEJHGSNY-UHFFFAOYSA-N 0.000 claims 1
- RMGHERXMTMUMMV-UHFFFAOYSA-N 2-methoxypropane Chemical group COC(C)C RMGHERXMTMUMMV-UHFFFAOYSA-N 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
- 239000000543 intermediate Substances 0.000 abstract description 23
- 150000004657 carbamic acid derivatives Chemical class 0.000 abstract description 5
- 239000002904 solvent Substances 0.000 description 43
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 39
- 239000000243 solution Substances 0.000 description 39
- 238000006243 chemical reaction Methods 0.000 description 34
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 30
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 26
- 239000000203 mixture Substances 0.000 description 26
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 13
- 239000007795 chemical reaction product Substances 0.000 description 11
- 238000006722 reduction reaction Methods 0.000 description 11
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 10
- 238000002360 preparation method Methods 0.000 description 10
- 230000009467 reduction Effects 0.000 description 10
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 229940093499 ethyl acetate Drugs 0.000 description 9
- 235000019439 ethyl acetate Nutrition 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 239000002253 acid Substances 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 8
- 238000001953 recrystallisation Methods 0.000 description 8
- 239000007858 starting material Substances 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- PFKFTWBEEFSNDU-UHFFFAOYSA-N carbonyldiimidazole Chemical compound C1=CN=CN1C(=O)N1C=CN=C1 PFKFTWBEEFSNDU-UHFFFAOYSA-N 0.000 description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 5
- 239000004480 active ingredient Substances 0.000 description 5
- 239000012074 organic phase Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- YOWQWFMSQCOSBA-UHFFFAOYSA-N 2-methoxypropene Chemical group COC(C)=C YOWQWFMSQCOSBA-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical group N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 4
- 229910000091 aluminium hydride Inorganic materials 0.000 description 4
- OLBWFRRUHYQABZ-MRVPVSSYSA-N carisbamate Chemical compound NC(=O)OC[C@@H](O)C1=CC=CC=C1Cl OLBWFRRUHYQABZ-MRVPVSSYSA-N 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 150000008282 halocarbons Chemical class 0.000 description 4
- 150000004678 hydrides Chemical class 0.000 description 4
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 4
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 4
- 238000000746 purification Methods 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
- 150000001721 carbon Chemical group 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 150000004702 methyl esters Chemical class 0.000 description 3
- 229920001843 polymethylhydrosiloxane Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000000634 powder X-ray diffraction Methods 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- PWMWNFMRSKOCEY-UHFFFAOYSA-N 1-Phenyl-1,2-ethanediol Chemical class OCC(O)C1=CC=CC=C1 PWMWNFMRSKOCEY-UHFFFAOYSA-N 0.000 description 2
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000002441 X-ray diffraction Methods 0.000 description 2
- 239000008186 active pharmaceutical agent Substances 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- 125000004104 aryloxy group Chemical group 0.000 description 2
- 238000003556 assay Methods 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 125000001246 bromo group Chemical group Br* 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000012512 characterization method Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229940126534 drug product Drugs 0.000 description 2
- 229940088679 drug related substance Drugs 0.000 description 2
- 239000012065 filter cake Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 229940052308 general anesthetics halogenated hydrocarbons Drugs 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 125000002883 imidazolyl group Chemical group 0.000 description 2
- 239000013067 intermediate product Substances 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 239000000825 pharmaceutical preparation Substances 0.000 description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 230000001376 precipitating effect Effects 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000012279 sodium borohydride Substances 0.000 description 2
- 229910000033 sodium borohydride Inorganic materials 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- ZUHZGEOKBKGPSW-UHFFFAOYSA-N tetraglyme Chemical compound COCCOCCOCCOCCOC ZUHZGEOKBKGPSW-UHFFFAOYSA-N 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- PYOKUURKVVELLB-UHFFFAOYSA-N trimethyl orthoformate Chemical compound COC(OC)OC PYOKUURKVVELLB-UHFFFAOYSA-N 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- IFNXAMCERSVZCV-UHFFFAOYSA-L zinc;2-ethylhexanoate Chemical compound [Zn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O IFNXAMCERSVZCV-UHFFFAOYSA-L 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical compound CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 1
- ZVAKZVDJIUFFFP-UHFFFAOYSA-N 2-chlorooxolane Chemical compound ClC1CCCO1 ZVAKZVDJIUFFFP-UHFFFAOYSA-N 0.000 description 1
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 1
- BTDQXGUEVVTAMD-UHFFFAOYSA-N 2-hydroxyethyl carbamate Chemical compound NC(=O)OCCO BTDQXGUEVVTAMD-UHFFFAOYSA-N 0.000 description 1
- ATVJJNGVPSKBGO-UHFFFAOYSA-N 3,4-dihydro-2h-thiopyran Chemical group C1CSC=CC1 ATVJJNGVPSKBGO-UHFFFAOYSA-N 0.000 description 1
- CSDQQAQKBAQLLE-UHFFFAOYSA-N 4-(4-chlorophenyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine Chemical compound C1=CC(Cl)=CC=C1C1C(C=CS2)=C2CCN1 CSDQQAQKBAQLLE-UHFFFAOYSA-N 0.000 description 1
- FSMHNRHLQAABPS-UHFFFAOYSA-N 4-methoxy-3,6-dihydro-2h-pyran Chemical compound COC1=CCOCC1 FSMHNRHLQAABPS-UHFFFAOYSA-N 0.000 description 1
- HJRITXIURQRVQY-UHFFFAOYSA-N 4-methoxy-3,6-dihydro-2h-thiopyran Chemical compound COC1=CCSCC1 HJRITXIURQRVQY-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical group NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 1
- XJUZRXYOEPSWMB-UHFFFAOYSA-N Chloromethyl methyl ether Chemical compound COCCl XJUZRXYOEPSWMB-UHFFFAOYSA-N 0.000 description 1
- 206010010904 Convulsion Diseases 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910017489 Cu I Inorganic materials 0.000 description 1
- BUDQDWGNQVEFAC-UHFFFAOYSA-N Dihydropyran Chemical compound C1COC=CC1 BUDQDWGNQVEFAC-UHFFFAOYSA-N 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- 238000012369 In process control Methods 0.000 description 1
- 208000019695 Migraine disease Diseases 0.000 description 1
- 208000007101 Muscle Cramp Diseases 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229910006124 SOCl2 Inorganic materials 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 208000005392 Spasm Diseases 0.000 description 1
- 208000006011 Stroke Diseases 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000003637 basic solution Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 125000001743 benzylic group Chemical group 0.000 description 1
- 150000003842 bromide salts Chemical class 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- SHZIWNPUGXLXDT-UHFFFAOYSA-N caproic acid ethyl ester Natural products CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 description 1
- WOYOQLVBGYGWQY-UHFFFAOYSA-N carbonic acid;1-phenylethane-1,2-diol Chemical compound OC(O)=O.OCC(O)C1=CC=CC=C1 WOYOQLVBGYGWQY-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 210000003169 central nervous system Anatomy 0.000 description 1
- 238000004296 chiral HPLC Methods 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 229960001701 chloroform Drugs 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 230000036461 convulsion Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000010511 deprotection reaction Methods 0.000 description 1
- 150000001354 dialkyl silanes Chemical class 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- NKDDWNXOKDWJAK-UHFFFAOYSA-N dimethoxymethane Chemical compound COCOC NKDDWNXOKDWJAK-UHFFFAOYSA-N 0.000 description 1
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 1
- POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 206010015037 epilepsy Diseases 0.000 description 1
- AZHSSKPUVBVXLK-UHFFFAOYSA-N ethane-1,1-diol Chemical compound CC(O)O AZHSSKPUVBVXLK-UHFFFAOYSA-N 0.000 description 1
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical class CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 125000005059 halophenyl group Chemical group 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 125000002962 imidazol-1-yl group Chemical group [*]N1C([H])=NC([H])=C1[H] 0.000 description 1
- 238000010965 in-process control Methods 0.000 description 1
- 150000004694 iodide salts Chemical class 0.000 description 1
- 125000002346 iodo group Chemical group I* 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000012280 lithium aluminium hydride Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical class COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 206010027599 migraine Diseases 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 208000004296 neuralgia Diseases 0.000 description 1
- 208000021722 neuropathic pain Diseases 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 125000000025 triisopropylsilyl group Chemical group C(C)(C)[Si](C(C)C)(C(C)C)* 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- PKJOUIVGCFHFTK-UHFFFAOYSA-L zinc;hexanoate Chemical compound [Zn+2].CCCCCC([O-])=O.CCCCCC([O-])=O PKJOUIVGCFHFTK-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
- C07C69/734—Ethers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/325—Carbamic acids; Thiocarbamic acids; Anhydrides or salts thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/12—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/14—Unsaturated ethers
- C07C43/178—Unsaturated ethers containing hydroxy or O-metal groups
- C07C43/1786—Unsaturated ethers containing hydroxy or O-metal groups containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
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- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The invention concerns a new process for preparing (S)-(+)-2-(substituted phenyl)-2-hydroxy-ethyl carbamates and to novel intermediates used in this process. It further relates to polymorphic forms of said carbamates and to processes for preparing said polymorphic forms.
Description
Process for preparing 2- (Substituted Phenyl) - 2- Hydroxy-ethyl Carbamates Brief description of the invention The present invention relates to a new process for preparing (S) - (+) - 2-(substituted phenyl) - 2- hydroxy-ethyl carbamates and to novel intermediates used in this process.
It further relates to polymorphic forms of said carbamates.
Bacl~~round of the 111vention 2- (Substituted phenyl) - 2- hydroxy-ethyl carbamates and their isomers have been described in US-5,698,588 and in US-5,854,283, which corresponds to WO-97/26241, as compounds useful for treating disorders of the central nervous system in particular convulsions, epilepsy, stroke, muscle spasms, neuropathic pain and migraine.
These compounds have an asymmetric carbon atom at the benzylic position, which is the aliphatic carbon atom adjacent to the phenyl ring. This asymmetric carbon atom preferably is in an S-configuration. A preferred compound among these carbamates is (S) - (+) - 2- (2-chlorophenyl) - 2- hydroxy-ethyl carbamate, which compound is also referred to as RWJ-333369. This and similar optically pure forms of carbamates of halogenated 2-phenyl-1,2-ethanediol have been described in US-6,127,412 and US-6,103,759.
These compounds are prepared by reacting the appropriately substituted phenyl-1,2-ethanediol with dimethylcarbonate thus yielding the corresponding phenyl-1,2-ethanediol carbonate which subsequently was reacted with a suitable amine which yielded two regioisomeric forms of the resulting carbamates which had to be separated by column chromatography. Stereoisomerically pure compounds were prepared similarly, starting from the enantiomerically pure starting material. This process results CONFIRMATION COPY
_2_ in a mixture of two regioisomeric products, one of which needs to be removed, which has a negative impact on the yield. Both regioisomeric end products are separated by chromatography which is a cumbersome procedure, especially in large scale production.
It is an object of this invention to provide a process that not only avoids this separation step and concomitant loss of undesired regioisomer, but also results in end product in high yield and purity, in particular in high enantiomeric purity. A further object is to provide a process that can be scaled up to large production batch sizes, to provide a process that uses starting materials that are easy to produce or are commercially available. It is still a further object to provide a process that is cost-effective and does not give rise to side products that are hazardous or difficult to remove. It is another obj ect of the present invention to provide a process that has a limited number of purification steps, in particular a process wherein some or all of the intermediates need 1S no purification. A still further object is to provide a process that avoids excess quantities of starting materials and solvents.
These objects are attained by the process of the present invention.
Drug substances, also referred to as active pharmaceutical ingredients, can occur as polymorphic forms. In almost all instances, a particular polymorphic form has different properties compared to the active ingredient not occurring in a specific polymorphic form or compared to another polymorphic form of an active ingredient.
Properties may differ as far as solubility, stability, flowability, tractability, compressibility, etc., are 2S concerned. These differences in turn are known to affect the properties of the formulations made of such active ingredients as well as the final or finished dosage forms thereof. Authorities responsible for drug approval in many countries require the complete characterization of the active ingredient used in each drug product, including the identification and control of polyrnorphic forms. If present in the finished product, drug approving authorities require the manufacturer of the active substance, in the least, to control its synthetic processes such that the percentages of the various respective polymorphic forms, when present, are consistent among batches and within the drug substance's approved specifications. Left uncontrolled in synthetic processes, the percentage of a given polymorph can fluctuate therefore having an effect of the properties of the active substance and the finished drug product such that it no longer meets the specifications of the drug approval. Therefore a robust control is required of the synthetic process specifications and of the end product, in particular as far as the presence of consistent amounts of polymorphic forms is concerned.
Many active substances do not show polymorphism and the presence of polymorphic forms of a new chemical active ingredient is not readily predictable.
Variations in the process parameters can lead to varying degrees of the presence of polymorphic forms in end products, which, as explained above is undesirable. Therefore the l~nowledge of the presence of polyrnorphic forms and their characterization is a highly desirable goal to achieve.
Quite unexpectedly it has now been found that (S) - (+) - 2- (substituted phenyl) - 2-hydroxy-ethyl carbamates occur as polymorphic forms that can be isolated and characterized. In an additional aspect, this invention provides practical and reproducible procedures to prepare these polymorphic forms.
Summary of the Tnvention The present invention relates to a process of preparing a compound of formula (~:
OH Ri O N\R2 R
wherein:
R is halo;
It further relates to polymorphic forms of said carbamates.
Bacl~~round of the 111vention 2- (Substituted phenyl) - 2- hydroxy-ethyl carbamates and their isomers have been described in US-5,698,588 and in US-5,854,283, which corresponds to WO-97/26241, as compounds useful for treating disorders of the central nervous system in particular convulsions, epilepsy, stroke, muscle spasms, neuropathic pain and migraine.
These compounds have an asymmetric carbon atom at the benzylic position, which is the aliphatic carbon atom adjacent to the phenyl ring. This asymmetric carbon atom preferably is in an S-configuration. A preferred compound among these carbamates is (S) - (+) - 2- (2-chlorophenyl) - 2- hydroxy-ethyl carbamate, which compound is also referred to as RWJ-333369. This and similar optically pure forms of carbamates of halogenated 2-phenyl-1,2-ethanediol have been described in US-6,127,412 and US-6,103,759.
These compounds are prepared by reacting the appropriately substituted phenyl-1,2-ethanediol with dimethylcarbonate thus yielding the corresponding phenyl-1,2-ethanediol carbonate which subsequently was reacted with a suitable amine which yielded two regioisomeric forms of the resulting carbamates which had to be separated by column chromatography. Stereoisomerically pure compounds were prepared similarly, starting from the enantiomerically pure starting material. This process results CONFIRMATION COPY
_2_ in a mixture of two regioisomeric products, one of which needs to be removed, which has a negative impact on the yield. Both regioisomeric end products are separated by chromatography which is a cumbersome procedure, especially in large scale production.
It is an object of this invention to provide a process that not only avoids this separation step and concomitant loss of undesired regioisomer, but also results in end product in high yield and purity, in particular in high enantiomeric purity. A further object is to provide a process that can be scaled up to large production batch sizes, to provide a process that uses starting materials that are easy to produce or are commercially available. It is still a further object to provide a process that is cost-effective and does not give rise to side products that are hazardous or difficult to remove. It is another obj ect of the present invention to provide a process that has a limited number of purification steps, in particular a process wherein some or all of the intermediates need 1S no purification. A still further object is to provide a process that avoids excess quantities of starting materials and solvents.
These objects are attained by the process of the present invention.
Drug substances, also referred to as active pharmaceutical ingredients, can occur as polymorphic forms. In almost all instances, a particular polymorphic form has different properties compared to the active ingredient not occurring in a specific polymorphic form or compared to another polymorphic form of an active ingredient.
Properties may differ as far as solubility, stability, flowability, tractability, compressibility, etc., are 2S concerned. These differences in turn are known to affect the properties of the formulations made of such active ingredients as well as the final or finished dosage forms thereof. Authorities responsible for drug approval in many countries require the complete characterization of the active ingredient used in each drug product, including the identification and control of polyrnorphic forms. If present in the finished product, drug approving authorities require the manufacturer of the active substance, in the least, to control its synthetic processes such that the percentages of the various respective polymorphic forms, when present, are consistent among batches and within the drug substance's approved specifications. Left uncontrolled in synthetic processes, the percentage of a given polymorph can fluctuate therefore having an effect of the properties of the active substance and the finished drug product such that it no longer meets the specifications of the drug approval. Therefore a robust control is required of the synthetic process specifications and of the end product, in particular as far as the presence of consistent amounts of polymorphic forms is concerned.
Many active substances do not show polymorphism and the presence of polymorphic forms of a new chemical active ingredient is not readily predictable.
Variations in the process parameters can lead to varying degrees of the presence of polymorphic forms in end products, which, as explained above is undesirable. Therefore the l~nowledge of the presence of polyrnorphic forms and their characterization is a highly desirable goal to achieve.
Quite unexpectedly it has now been found that (S) - (+) - 2- (substituted phenyl) - 2-hydroxy-ethyl carbamates occur as polymorphic forms that can be isolated and characterized. In an additional aspect, this invention provides practical and reproducible procedures to prepare these polymorphic forms.
Summary of the Tnvention The present invention relates to a process of preparing a compound of formula (~:
OH Ri O N\R2 R
wherein:
R is halo;
R1 and R2 independently are hydrogen or Ci_4alkyl, optionally substituted with phenyl or substituted phenyl, wherein substituted phenyl has substituents selected from halogen, C1_4alkyl, Cl_4alkyloxy, amino, nitro and cyano;
characterized by (a) reducing an ester of formula:
OP
I ~ \COzRs R
(B) wherein:
P is an appropriate alcohol-protecting group;
R3 is C1_4alkyl;
with an appropriate ester-to-alcohol reducing agent, thus obtaining an alcohol of formula:
OP
I ~ ~CH20H
R
(~) (b) reacting the alcohol of formula (~ with a carbonyl compound of formula O
X Y
wherein X and Y are appropriate leaving groups; and subsequently with an amine of formula a H N
R
(V) thus obtaining a compound of formula:
OP Rl O N~Ra R
(V~;
(c) removing the protecting group P thus obtaining a compound of formula (l~.
In some instances one or more of the substituents Rl, R2 and R3 may have asymmetric carbon atoms and hence may cause the compounds of formula (~ to occur in stereoisomeric forms. Such stereoisomeric forms are intended to be embraced within the scope of the present invention.
Preferred compounds of formula (n are those wherein R is 2-chloro, Rl and R2 are _ hydrogen. .. , The group P is an appropriate alcohol protecting group. Preferred groups P are of the ether type. A particularly preferred protecting group P is 2-(2-methoxy)propyl.
In a preferred execution of the process the carbonyl compound of formula (IV) is selected from 1,1 '-carbonyl-diimidazole and phenyl chloroformiate.
A particular execution of the process is that wherein R3 is methyl.
Another particular execution of the process is that wherein the appropriate ester-to-alcohol reducing agent is a metal hydride or a complex metal hydride.
In a further aspect the invention relates to a compound of formula OP Rl O N~Ra I
wherein R, Rl and RZ are as defined in claims 1 or 2 and P is an appropriate hydroxy-protecting group.
In another aspect, the invention relates to a compound of formula OP
I ~ ~CHZOH
. ~R I
wherein R is as defined in claims 1 or 2 and P is an appropriate hydroxy-protecting group.
In still another aspect the invention relates to a compound of formula OP
I ~ ~CO2R3 R
wherein R is as defined in claims 1 or 2, R3 is C1_4all~yl; and P is an appropriate hydroxy-protecting group.
Preferred are those compounds of formulae (IV), (111) or (II) wherein P is 2-(2-methoxy)propyl.
Also preferred are those compounds of formula (II) wherein R3 is methyl.
In still another aspect, the invention relates to a process for preparing a compound of formula (VI) characterized by process steps (a) and (b) as outlined above.
In still another aspect, the invention relates to a process for preparing a compound of formula (111] characterized by process step (a) as outlined above.
_g_ In still another aspect, the invention relates to a process for preparing a compound of formula (II) characterized by process steps (d) and (e) as outlined hereinafter.
The invention further provides a process preparing a compound of formula (I) characterized byprocess steps (d) and (e) as outlined hereinafter and by process steps (a), (b) and (c) as outlined above.
In a further aspect, this invention concerns the presence of polymorphic forms of the (S) - (+) - 2- (substituted phenyl) - 2- hydroxy-ethyl carbamates. In particular it concerns two polymorphic forms of the compound 2-(2-chlorophenyl)-2-(2-(2-methoxy)propyl)-ethyl carbamate The invention also concerns processes for preparing these new polymorphic forms.
Detailed Description of the Invention Subject of the present invention is a process for preparing compounds of formula (I), as outlined above, and the intermediates of formula (II), (III), (IV), and (V) as represented and defined hereinabove.
Preferred are those compounds and intermediates as defined herein wherein R is chloro, Rl and R2 are hydrogen. The compound of formula (I) wherein the substituents have the latter meanings is also referred to as 'RWJ-333369' and can be represented by the structural formula:
Cl OH
O NHZ
(I-a) The term "halogen" refers to fluoro, chloro, bromo and iodo.
"Cl_4alkyl" defines straight and branched chain saturated hydrocarbon radicals having from 1 to 4 carbon atoms such as methyl, ethyl, 1-propyl, 2-propyl, 1-butyl, 2-butyl, 2-methyl-1-propyl, 2-methyl-2-propyl. , "C1_4alkyloxy" defines C1_4alkyl radicals linked to an oxygen atom such as methoxy, ethoxy, 1-propoxy, 2-propoxy, 1-butoxy, 2-butoxy and the lilce.
"Substituted phenyl" is phenyl being substituted with the substituents outlined above.
Preferably, substituted phenyl has 1, 2 or 3 substituents. A preferred substituent is halogen, more preferably chloro.
P, as mentioned above, is an appropriate hydroxy protecting group. Preferably it should be selected such that it is stable in the reduction procedure of (In to (ffl]
as well as the subsequent reaction step from (III] to (Vn. The preferred reduction procedure being with complex hydrides as outlined hereinafter, the group P should be stable towards these complex hydrides and the reaction products therefrom. The reduction with complex hydrides requires basic conditions and hence the group P should not be cleaved in these basic conditions. The group P should preferably be removable under acidic conditions which should be such that the carbamate function is not split.
Particularly preferred are protecting groups P that are removable at a pH
which is about 1 or slightly higher.
Particularly useful are groups P of the ether type. As examples of P there may be mentioned:
methoxymethyl ethers (MOM): which can be prepared from methoxymethylchloride or formaldehyde dimethylacetal;
tetrahydropyran ethers (THP ethers) prepared from dihydropyran;
tetrahydrothioypyranyl ethers from dihydrothiopyran;
chloro substituted tetrahydrofuranyl ethers from 2-chlorotetrahydrofuran;
tetrahydrothiofuranyl ethers from dihydrothiofuran;
1-ethoxyethyl ethers from ethylvinyl ethers or 1-ethoxyethyl chloride 1-methyl-1-methoxyethyl ethers from methylvinyl ethers, which are of particular interest;
triphenyl ethers and appropriate derivatives thereof which can be prepared from the corresponding.chlorides;
benzyl ethers and appropriate derivatives thereof which can be prepared from the corresponding bromides or iodides;
4-methoxytetrahydropyranyl ethers from 5,6-dihydro-4-methoxy-2H-pyran;
4-methoxytetrahydrothiopyranyl ethers from 5,6-Dihydro-4-methoxy-2H
thiopyran.
It is furthermore advantageous to use such groups P which do not lead to a mixture of diastereomers, i.e. P groups without an asymmetric center. Under certain circumstances, e.g. depending upon the nature of the reducing agent, particular silyl ethers can be used as appropriate groups P, in particular t.butyldimethylsilyl (TBDMS), triisopropylsilyl, tribenzylsilyl, and the like.
Step (ay preparation of 2-(substituted phenyl)-2-(protected hydroxyl-ethanol (IIP
According to the first step of the process of this invention, the ester (In is reduced to the corresponding alcohol of formula (III) using an appropriate ester-to-alcohol reducing agent. The latter may be a metal hydride or a complex metal hydride such as lithium aluminium hydride or derivatives thereof.
Particular reduction agents for this reaction are silane agents such as trialkylsilanes, dialkylsilanes, trialkoxysilanes and preferably poly methylhydrogensiloxane ('PMHS') in the presence of a suitable catalyst. The latter in particular are transition metal halogenides or carboxylates, and preferably the latter is a zinc carboxylate, such as zinc hexanoate or a derivative thereof, more preferably zinc 2-ethylhexanoate, in the presence of a metal hydride such as an alkali metal or earth alkaline metal hydride, or aluminium hydride, e.g. lithium, sodium, potasium, calcium hydride, or a complex hydride such as a borohydride or aluminium hydride, in particular an alkali metal borohydride or aluminiumhydride, e.g. lithium, sodium or potassium borohydride or aluminium hydride. A combination of zinc 2-ethylhexanoate and sodium borohydride is most preferably used as the catalyst mixture. These and similar reduction agents are described in Patent Application WO 96112694 (1995) and in J. Ulinan, The Alefnbic, 1999, 59, 1 ff.
The reaction of this process step is conducted in a suitable solvent, e.g. an ether or polyether, or a hydrocarbon, in particular an aromatic hydrocarbon. Specific examples of suitable solvents comprise diethyl ether, dipropyl ether, diisopropyl ether, dibutyl ether, diglyme and toluene.
The reduction agent can be formed by stirring a mixture of the agents ERS A
and ERS
B in a separate reaction vessel (ERS = Ester Reduction System), commercially available from Rohm & Haas). ERS A is a solution of NaBH4 in tetraglyme, whereas ERS B is a solution of Zn(carboxylate)2*HZO, in particular of Zn(2-ethylhexanoate)Z
*H20, in tetraglyme. ERS A and ERS B are preferably mixed at higher temperature, e.g. at a temperature in the rage of 50 to 90°C, in particular at 70°C for a period of several minutes, e.g. for 30 min. Subsequently the ERS A and ERS B mixture is added to the ester (Ilk and ERS C is added. ERS C is poly methylhydrogensiloxane.
The reducing agent can also be generated ira situ in the reaction vessel, which is particularly attractive. In this variant, intermediate (In is dissolved in a suitable solvent, preferably in toluene at increased temperature of 80-90°C. ERS
B is added first in one portion, followed by the addition of ERS A also in one portion. Then immediately ERS C is added within one hour while controlling the temperature and keeping it at higher temperature, in particular around 95°C.
The starting mandelic acid ester (In is prepared as described hereinafter and can be isolated and optionally purified and used as such in the reduction step. The ester (Il) can also be kept dissolved in the solvent in wluch it was prepared and used as such in the reduction step.
Preferably the substituted mandelic acid ester (I~ is a methyl ester.
In a particular execution of this process step the starting ester (I~ is either used dissolved in the solvent of the previous reaction step, or it can also be solved in a suitable solvent, such as for example an ether, e.g. in di-n-butylether, or preferably in toluene. The reducing agent, prepared as above, is added in one portion to the solution, followed by the addition of ERS C within one hour. The reaction mixture optionally can be heated to 90°C prior to addition of ERS C. Then the temperature is increased to 90°C and kept at that temperature until an in-process-control shows a conversion of at least 99%. The reaction time is around 1 h. After complete reduction the mixture is cooled to 15 to 20°C and hydrolyzed carefully first with methanol and subsequently with aqueous alkali metal hydroxide solution, which preferably is a NaOH
solution in slight excess (e.g. 1.3 mol-eq., using a 30% solution).
Subsequently, the mixture is refluxed for about 1 h at about 50°C and the layers are separated at room temperature. The organic layer is washed with water and with saturated aqueous NaCI at room temperature.
The quantity of ERS C is in the range of 2 to 4, in particular in the range of 2.2 to 3 molar equivalents, preferably 2.3 molar equivalents of ERS C are used.
The reaction typically is complete after about 1 hour.
After completion of the reduction reaction, the excess of ERS C can be destroyed with a suitable ester, in particular with ethyl acetate. After addition of the said ester, the mixture is stirred for one hour and hydrolyzed at 90°C by addition of aqueous base solution, preferably a NaOH or a KOH-solution (e.g. of 33%) and further preferably with the use of methanol. Further work-up comprises the separation of the organic layer and washing with aqueous basic solution (e.g. I~OH-solution of 33%) and with water.
The resulting methylester is an oil, and, if desired, can be distilled for purification.
Step (b)' preparation of 2-(substituted phenyl)-2-(protected hydroxyl-ethyl carbamate (VP
W this step the alcohol of formula (~ is reacted with a carbonyl compound of formula O
X ~Y
wherein X and Y are appropriate leaving groups. Preferably one of X or Y is more reactive than the other. X and Y can be halogen, in particular chloro or bromo, but preferably X and Y are imidazolyl groups. If X is halo, Y preferably is an aryloxy or alkoxy group. In the latter instance (V) is an alkyl or aryl halo formiate.
Particular aryl groups in (TV) are phenyl or substituted phenyl, e.g. halophenyl, or C1_4 alkyl. A
preferred example of (IV) is phenyl chloroformiate or l, l '-carbonyl-diimidazole.
The reaction is conducted in a suitable solvent such as a hydrocarbon, in particular an aromatic hydrocarbon, e.g. toluene, or in an ether, e.g. THF. The reaction temperature depends upon the reactivity of the reagent (IV) but in general is room temperature or lower. In case N,N'-carbonyl diimidazole is used as reagent the reaction preferably is conducted at room temperature (i.e.. at about 25 °C).
The reaction typically is complete after less than 1 hour, e.g. after about %2 hour. The reaction product of this reaction is usually not isolated; it can be represented by the following formula:
OP
O Y
R
O
(~-a) wherein Y is as defined hereinabove and in particular is an imidazolyl group, or an aryloxygroup, e.g. a phenoxy or substituted phenoxy group. The intermediates of formula (IV-a) are deemed novel and constitute an additional feature of the present invention. Preferred intermediates of formula (IV-a) are those wherein Y is imidazol-1-yl.
The product of he previous reaction, i.e. the intermediate of formula (IV-a), is usually not isolated and is reacted immediately with the amine of formula (V) as specified above. A preferred amine is ammonia, but it can also be an ammonium salt. In that instance the ammonia or an ammonium salt is in an aqueous medium and added to the solution of intermediate (IV-a) at room temperature.
Vigorous stirring is recommended when using (V) in aqueous media, because of the two phase system. The reaction is terminated after several hours, in particular after about 4 hrs. The organic phase is separated and the product can optionally be isolated and purified. The organic phase with product (VI) dissolved therein can also be used as such in the subsequent reaction step.
Ste~c~ preparation of 2-(substituted phenyl)-2-hydroxyethyl carbamate (I) This reaction step involves the deprotection of the hydroxy function and depends on the nature of the group P.
Where P is 2-methoxy-2-propyl, removal is by addition of an appropriate acid, e.g.
hydrochloric acid.
In a preferred execution, product (VI) is used dissolved in the solvent of the previous step. Water and concentrated hydrochloric acid are added while stirnng.
Already after a few minutes the reaction is almost completed and the end procuct (I) starts precipitating. The reaction mixture is stirred for a couple of hours, in particular for about 4 hours because in this Way the end product can be filtered better.
Subsequently the end product is filtered off and washed.
The end product (I) can be recrystallized from a suitable solvent such as an alcohol, e.g.
methanol, preferably with addition of acidified water.
Starting materials The starting materials(I~ are obtained by a process which is characterized by:
(d) an esterification reaction of an appropriately substituted mandelic acid of formula:
OH
I ~ ~COOH
R
(V
thus preparing the corresponding ester of formula OH
~COOR3 R
(~) wherein in (VIII) and (IX) R and R3 are as defined above and R preferably is 2-chloro and/or R3 preferably is methyl; and (e) treating the ester (IX) with a suitable reagent generating a hydroxy protecting group, thus preparing an intermediate of formula OP
~COOR3 R
i (~
wherein R and P are as defined above.
The ester (IX) is reacted with an appropriate agent capable of introducing a hydroxy protecting group. A preferred agent is 2-methoxypropene.
Alternatively, the sequence of the above steps may be switched, i.e. the hydroxy protecting group may be introduced and subsequently the ester formed.
Step (d): Preparation of substituted mandelic acid esters (IX) According to this reaction step the starting acid (V~ is reacted in the alcohol of which IS the ester (IX) is derived. Typically a C1_4 alkanol is used, preferably methanol, thus yielding the corresponding C1_4 alkyl esters or preferably the methyl ester of (VITI).
The reaction is conducted with an excess of a strong acid, preferably a hydrohalic acid such as HCl, in particular with 1-4 molar equivalents, preferably with 2.5 molar equivalents of concentrated HCI. The reaction also works with a catalytic amount of sulfuric acid or also with SOCl2 . In the latter instance the reaction is highly exothermic, requiring appropriate measures for controlling the temperature.
The reaction preferably is conducted at room temperature or slightly increased temperatures, preferably not higher than about 30°C. The reaction time usually is less than about 1 hour, e.g. about 30 min. The resulting ester (IX) typically is an oily compound which is used as such in the subsequent process steps. In a preferred execution, the ester (IX) is kept in the solvent in which it was made and is used further dissolved in this solvent.
Step (ey Preparation of h~~protected substituted mandelic acid esters (ll~.
The reaction conditions of this step depend on the nature of protecting group P.
_ In a preferred execution, P is 2-methoxy-1-propyl which is derived from 2-methoxypropene. The latter is dissolved in a suitable solvent, in particular the solvent in which the other reaction steps are conducted. This solution is added to a solution of intermediate (IX) in a suitable solvent which has been acidified, e.g. by addition of hydrochloric acid, in particular by adding gaseous hydrochloric acid over the solution. The pH should preferably be low, e.g. pH 1-2. The solvent of intermediate (IX) should preferably be the same as that wherein the 2-methoxypropene is dissolved and more preferably should be the same as the solvent used in the other reaction steps.
The reaction is complete in less than 1 hour, normally witlun half an hour.
The process according to the present invention yields the end product (n in high yield and purity and can be scaled up to production size batches. A particular aspect of the current process is that it leaves the stereochemical integrity intact of the asymmetric center on the carbon atom bearing the hydroxy function, i.e. the present process shows neglectable or no racemisation.
The various intermediate products of the process, including the steps for preparing the starting materials, can be isolated and if desired further purified before further use in a next step. Alternatively, all the process steps, if desired also including the steps for preparing the starting materials, can be conducted in the same solvent, i.e.
without isolation and optional purification of the intermediate products. In the latter instance it may be advantageous to distil off some of the solvent or to add some of it during one or more of the reaction steps. A suitable solvent for the one solvent execution of the process is an aromatic hydrocarbon, preferably toluene. It is also possible to conduct a certain number of steps in one solvent and the others in another.
Conducting the whole process in one solvent has the particular advantage that the process is much simpler and can be conducted more quickly without having to discard or recuperate solvents, which is advantageous economically as well as from an enviromnental aspect.
_ Pol,>~rphs The present invention is further directed to novel crystalline structures of the compound of formula (I) wherein R is 2-chloro, Rl and R2 are hydrogen, said compound hereinafter being referred to as compound (I-a).
The crystalline forms of compound (I-a) may be prepared by an appropriate recrystallization of compound formula (I-a) from a suitable organic solvent.
Depending upon the recrystallisation procedure either form A or form B can be obtained.
One crystalline form of compound (I-a) is referred to as 'form A' and is prepared by recrystallisation of compound (I-a) from a suitable solvent. The temperature in this recrystallisation procedure is kept below 60 °C, in particular below 50 °C. Suitable solvents are those wherein the compound of formula (I-a) dissolves at higher temperature and is relatively poorly soluble at lower temperature, e.g. at a temperature lower than 20 °C, or lower than 10 °C, or even lower than 0 °C, or -10 °C. Suitable solvents are the lower alkanols, i.e. the C1_4alkanols and in particular methanol.
In one type of embodiment, the compound (I-a) is dissolved by heating or refluxing in methanol, or by heating in a lower alkanol. The temperature of the mixture should not allowed to exceed 60 °C. Subsequently, the solution is cooled, preferably slowly, e.g.
by simply allowing the solution to cool. At a temperature of about 50 °C crystallization already starts. The mixture is stirred at room temperature for 15-20 hours whereupon acidified water is added. The water preferably is acidified with a strong acid, e.g.
hydrochoric acid or a similar acid to a pH value of about 3 to 4, in particular about pH
3.5. The mixture is further cooled to about 0 to 10 °C, in particular to about 5 °C and stirred at that temperature for a sustained period of time, e.g. about 1 hour.
The crystalline end product is then filtered and dried.
In a further aspect the present invention concerns the compound (I-a) predominantly in Form A. The invention in particular concerns compound (I-a) occurring as a polymorph mixture, which predominantly contains Form A. More in particular the invention concerns compound (I-a), occurring as polymorph mixture containing at least 90 % or _ more of form A, further in particular 95 % or more of Form A, still further in particular 99 % or more of Form A.
Hence, recrystallization of the compound of formula (I-a) as described above yields a novel crystalline form of (I-a), herein referred to as 'Form A'.
Compound (I-a) in Form A has a particular crystalline form, i.e. the monoclinic crystalline form.
One crystalline form of compound (I-a) is referred to as 'form B' and is prepared by recrystallisation of compound (I-a) from a suitable solvent. The temperature in this recrystallisation procedure is brought above 60 °C, in particular above 70 °C. Suitable solvents are those wherein the compound of formula (I-a) dissolves at higher temperature and is relatively poorly soluble at lower temperature, e.g. at a temperature lower than 20 °C, or lower than 10 °C, or even lower than 0 °C, or -10 °C. Suitable solvents are the lower alkanols, e.g. the C3_4alkanols and in particular propanol (n-propanol or 2-propanol). Other suitable solvents are esters such as ethyl acetate or a similar solvent, or mixtures thereof with lower boiling halogenated hydrocarbons such as trichloromethane or dichloromethane, which is preferred. In this instance, preferably, the starting material is first dissolved in the ethyl acetate after which the halogenated hydrocarbon is added. The volume of halogenated hydrocarbon that is used is equal to about five times (v/v) relative to the volume of ethyl acetate, preferably the volume ratio is in the range of about 1 : 2 to about 1: 5, e.g. it can be about 1 : 3 (ethylacetate halogenated hydrocarbon). Still further suitable solvents are polyols, in particular the glycols such as ethylene glycol, which is preferred, or propylene glycol, butylene glycol and the like. Water can be added, in particular where polyols are used as a solvent. If water is added, it may be acidified with a suitable strong acid such as hydrochloric acid to low pH, e.g. a pH which is in the range of pH 2 - 5, e.g. a pH which is about pH 3.
Water can be added in various quantities. For example where ethylene glycol or similar glycols are used, the volume ratios of glycol to added water are in the range of 1 : 1 to about 1 : 8, or 1 : 2 to 1 : 5, e.g. about 1 : 4 (glycol : water, v/v).
In one type of embodiment, the compound (I-a) is dissolved by heating or refluxing in 2-propanol, ethyl acetate or a mixture of ethylacetate/dicloromethane, more preferably a 1: 3 mixture of ethylacetate/dichloromethane. Subsequently the solution is allowed to cool whereupon the desired product crystallizes.
This procedure can also be used to convert form A into form B, i.e. by replacing the compound (I-a) by form A in the above procedure.
Form B can also obtained in a highly pure form by heating form A to 130°C over a period of 60 min (DSC experiment) as triclinic crystals.
In a further aspect the present invention concerns the compound (I-a) predominantly in Form B. The invention in particular concerns compound (I-a) occurring as a polymorph mixture, which predominantly contains Form B. More in particular the invention concerns compound (I-a) occurring as polymorph mixture containing at least 90 % or more of form B, further in particular 95 % or more of Form B, still further in particular 99 % or more of form B.
The novel crystalline forms of the compound of formula (I-a) may be characterized by their respective X-ray powder diffraction patterns utilizing appropriate powder diffractometers, in particular using the methodology as outlined in the Examples.
In a further aspect, this invention provides a process for preparing form A of the compound of formula (I-a), or the compound of formula (I-a) predominantly in form A, said process comprising dissolving the compound of formula (I-a) in a suitable solvent, heating the solvent to a temperature which is lower than about 60 °C
and higher than about 50 °C, and subsequently allowing to cool said solution. Suitable solvents are alcohols, in particular C1_~ alkanols, preferably methanol. In a particular execution of this process, the heated solution is allowed to cool until the first crystals appear, in particular the solution is allowed to cool to about 50 °C allowing the appearance of the first crystals, and subsequently allowed to cool further, in particular to room temperature.
In another aspect, this invention provides a process for preparing form B of the compound of formula (I-a), or the compound of formula (I-a) predominantly in form B, said process comprising recrystallisation of compound (I-a) from a suitable solvent at a temperature of 60 °C or higher, in particular of 70 °C or higher. Suitable solvents are, for example, the lower alkanols, e.g. the C3_4alkanols and in particular propanol. Other suitable solvents are ethyl acetate or mixtures thereof with lower boiling halogenated hydrocarbons such as dichloromethane.
The following Examples describe the invention in greater detail and are intended to illustrate the invention, but not to limit it.
Examples Preparation of (~-(+)-2-(2-chlorophenyl)-2-hydroxy-ethyl carbamate (compound (I-a)) Example 1 (,.5~-(+)-2-Chloromandelic acid methyl ester (Intermediate 1) (,$~-(+)-2-Chloromandelic acid (100.0 g, 535.9 mrnol) is dissolved at rt in methanol (553.0 g). After cooling to 10 ~ 5°C, hydrogen chloride gas (55.3 g) is conducted over the solution for 30 min holding the temperature below 25 ~ 5°C. The course of this reaction and the following reactions is followed by HPLC. Trimethyl orthoformate (62.6 g, 589.5 mmol) is added at 20~5°C to the colorless to light yellow solution which is stirred for 30 min at the same temperature. Thereafter the solvent and the hydrogen chloride gas is removed as far as possible irz vacuo (40 ~ 5°C, 40 ~ 10 mbar). The oily residue is diluted with toluene (130 g) and the solvent is removed again as far as possible in vacuo. Toluene (261 g) is added and the solution is cooled to 15 ~
5°C.
Example 2 2-Methoxy-1-proRyl derivatized (~-(+)-2-Chloromandelic acid methyl ester (Intermediate 2) Hydrogen chloride gas (0.55 g, 15 mmol) is conducted over the solution (pH-value drops from 3 to 1-2). In a second flash, 2-methoxy-propene (78.0 g, 1081.7 mmol) is dissolved in toluene (120 g) at 20 ~ 5°C and the above prepared solution of Intermediate 1 is added at a temperature range of 25~5°C (ca. 30 min).
After the addition is complete, the mixture is stirred for 30 min. Triethylamine (14.0 g, 138.3 mmol) is added to the colorless to light yellow solution, it is stirred at rt for 5 min and diluted with toluene (402 g) (pH >_ 8, if not, addition of triethylamine). The mixture is washed with water (1 x 150 g), aq. sodium hydrogencarbonate solution (5%, 1 x g), and aq. sat. sodium chloride solution (1 x 150 g). Drying with sodium sulfate (ca. 65 g), filtration, and removal of ca. 86 g toluene ih vacuo leads to Intermediate 2.
Example 3 2-(2-Chloro~henyl)-2-~2-(2-methoxy)propyl)-ethanol (Intermediate 3) At first VenpureTM ERS B (13.0 g) and secondly VenpureTM ERS A (13.0 g) is added and the mixture is heated within 45 min to 85~5°C. The appearance of the solution turns from clear to slightly cloudy. VenpureTM ERS C (73.9 g, ca. 1239.4 mmol) is dropped into the solution in such a way that the temperature is 95 ~5° C (ca. 45 min, delay of the start of the exothermic reaction is possible). The reaction is finished 15 min after the end of the dropping which is also indicated by an additional milky to gray (from zinc) appearance in the mixture. If not, an additional 7.0 g of each VenpureTM ERS B and VenpureTM ERS A are added directly to the reaction mixture and the whole is heated until the conversion is complete. The solution is cooled to 15 ~ 5°C and methanol (30 g) is added (hydrogen evolution). Aqueous sodium hydroxide solution (30%, 238.0 g) is added dropwise while holding the temperature below 20°C (ca. 30 min, above 25°C, a violent foaming is observed). After the addition is finished the two phase mixture is heated for 1 h to 50 ~
5°C, and the previously formed precipitate dissolves now. The phases are separated after cooling to-rt and the colorless organic phase is washed with water (1 x 200 g) and with aq. sat.
sodium chloride solution (1 x 200 g). Drying with sodium sulfate (ca. 65 g), filtration, and removal of ca. 180 g solvent in. vacuo gives a solution of Intermediate 3.
Example 4 2-(2-chlorophenyl)-2-(2-(2-methoxy)propyll-ethyl carbamate (Intermediate 5) To the solution obtained in example 3, a slurry of 1,1 '-carbonyl-diimidazole (103.8 g, 641.4 mmol) in toluene (180 g) is added within 30 min. at a temperature in the range of 25~5°C. The conversion to 1-imodazolyl-1' - [2- (2-chlorophenyl) -2 -[2- (2-methoxypropyl]- ethoxy carbonyl (Intermediate 4) is then complete.
Toluene (200 g) and aq. ammonium hydroxide solution (25%, 364 g) are added.
After 3 h vigorous stirring at rt, the phases are separated and the organic phase containing Intermediate 5 is washed with water (1 x 200 g) and with aqueous saturated sodium chloride solution (1 x 200 g).
Example 5 Preparation of Compound (I-a) To the organic phase containing Intermediate 5, prepared as described above, is added water (160 g) and conc. aq. hydrochloric acid (39 g) generating a pH-value <1Ø
Compound (I-a) starts precipitating while stirring after 5 min at rt. After 4 h, the product is filtered off, the filter cake is washed with water (3 x 75 g) and with toluene (3 x 44 g). 96.9 g compound (I-a) (purity 99.8%, assay 99.0% determined by HPLC, ee >99.9% determined by chiral HPLC , 444.8 mmol, overall yield 83.0%) after drying (50~5°C, 40~10 mbar).
Example 6 Preparation of Form A of Compound (I-a) This material of the previous example is suspended in methanol (115 g) and after heating to reflux, the formed solution is hot filtered, cooled to rt, and stirred for 15-20 h at this temperature. Water (577 g) containing aq. cone. hydrochloride acid (ca. 13 mg, pH-value of the solution is 3.70.2) is added. The mixture is cooled to 5~5°C, stirred for 2 h at the same temperature, and then filtered. The filter cake is washed with water (3x 30 g). After drying (50~5°C, 50~10 mbar), 93.0 g of Form A of comRound (I-a) (purity 100%, assay 99.7%, ee >99.9%, 430.0 mmol, overall yield 80.2%) is obtained as colorless needles.
Example 7 Determination of pol~nnorphic form b~powder X-ray diffractometry Sample preparation About 0.5 to 1 g of sample is gently pressed into a powder sample holder in order to get a well defined, smooth surface.
Instrument A computer controlled powder diffractometer system APD1700 (Philips) with an automated divergence slit and secondary monochromator or equivalent equipment is used.
Recording conditions Copper radiation: Kal = 0.15406 and K~ = 0.15444 nm Voltage: 40 kV
Current: 30 mA
Divergence slit: automated Receiving slit: 0.1 °
Graphite secondary monochromator for Cu-I~°,1 Xe proportional counter Counting starts at 1.5° 20 and proceeds in steps of 0.02° 20 to reach 40° 20. The counting time per interval is 3 sec and the total recording time is 2 h 50 min.
Form A of the compound of formula (I-a) may be characterized by its X-ray diffraction pattern, which comprises the major pealcs as listed in the Table 1 in the Examples.
TABLE 1. FORM A POWDER X-RAY DIFFRACTION PEAKS
Form B of the compound of formula (11) may be characterized by its X-ray diffraction pattern, which comprises the major peaks as listed in Table 2.
Form A
Angle d value Intensity 2-Theta Angstrom Cps 9.217 9.58681 4610 100.0 10.506 8.41395 108 2.3 14.954 5.91952 986 21.4 17.375 5.09990 1501 32.6 18.435 4.80892 3287 71.3 20.028 4.42979 884 19.2 20.720 4.28343 286 6.2 21.045 4.21801 2535 55.0 22.205 4.00026 80.1 1.7 23.257 3.82165 1248 27.1 24.954 3.56544 494 10.7 25.715 3.46166 1776 38.5 26.093 3.41233 684 14.8 27.379 3.25489 3953 85.8 27.689 3.21908 954 20.7 29.339 3.04172 163 3.5 30.134 2.96333 517 11.2 31.480 2.83961 129 2.8 31.780 2.81347 310 6.7 32.139 2.78287 113 2.4 32.880 2.72180 318 6.9 33.097 2.70446 337 7.3 34.664 2.58570 479 10.4 35.170 2.54967 972 21.1 35.500 2.52667 464 10.1 35.995 2.49305 109 2.4 36.700 2.44679 250 5.4 36.958 2.43029 374 8.1 37.314 2.40791 1034 22.4 38.349 2.34527 408 8.9 39.222 2.29508 161 3.5 39.683 2.26945 310 6.7 Example 8 Preparation of Form B of Compound (I-al 5.0 g (19.0 mmol) raw RWJ-333369 (polymorph A) is dissolved in 4.75 g 2-propanol by heating to reflux. This solution is cooled to room temperature within 30 min whereby the substance crystallizes. After additional stirring at 4°C
for 1 h, the product is filtered off and dried at 80°C and 20 mbar for 8h. Yield: 4.0 g (15.2 mmol, 80%) polymorphic form B.
2-Theta d-value Intens. Rel.Int.
9.13 9.686 486.0 0.324 10.38 8.522 198.0 0.132 12.81 6.910 334.0 0.223 15.04 5.890 507.0 0.338 15.92 5.567 153.0 0.102 17.32 5.120 594.0 0.396 18.31 4.845 694.0 0.463 18.58 4.775 282.0 0.188 19.37 4.582 239.0 0.159 20.04 4.431 326.0 0.217 20.81 4.268 864.0 0.576 21.72 4.092 324.0 0.216 22.15 4.013 1500.0 1.000 23.25 3.826 661.0 0.441 24.94 3.570 416.0 0.277 25.64 3.474 516.0 0.344 27.20 3.278 1044.0 0.696 27.59 3.233 506.0 0.337 28.23 3.161 216.0 0.144 28.56 3.125 221.0 0.147 29.44 3.034 208.0 0.139 30.34 2.946 328.0 0.219 30.83 2.900 314.0 0.209 31.77 2.816 259.0 0.173 32.13 2.786 200.0 0.133 32.68 2.740 335.0 0.223 33.04 2.711 276.0 0.184 _28_ 34.30 2.614 207.0 0.138 34.81 2.577 621.0 0.414 35.29 2.543 244.0 0.163 35.91 2.501 243.0 0.162 36.36 2.471 189.0 0.126 37.08 2.424 412.0 0.275 37.66 2.388 349.0 0.233 38.55 2.335 431.0 0.287 39.09 2.304 321.0 0.214
characterized by (a) reducing an ester of formula:
OP
I ~ \COzRs R
(B) wherein:
P is an appropriate alcohol-protecting group;
R3 is C1_4alkyl;
with an appropriate ester-to-alcohol reducing agent, thus obtaining an alcohol of formula:
OP
I ~ ~CH20H
R
(~) (b) reacting the alcohol of formula (~ with a carbonyl compound of formula O
X Y
wherein X and Y are appropriate leaving groups; and subsequently with an amine of formula a H N
R
(V) thus obtaining a compound of formula:
OP Rl O N~Ra R
(V~;
(c) removing the protecting group P thus obtaining a compound of formula (l~.
In some instances one or more of the substituents Rl, R2 and R3 may have asymmetric carbon atoms and hence may cause the compounds of formula (~ to occur in stereoisomeric forms. Such stereoisomeric forms are intended to be embraced within the scope of the present invention.
Preferred compounds of formula (n are those wherein R is 2-chloro, Rl and R2 are _ hydrogen. .. , The group P is an appropriate alcohol protecting group. Preferred groups P are of the ether type. A particularly preferred protecting group P is 2-(2-methoxy)propyl.
In a preferred execution of the process the carbonyl compound of formula (IV) is selected from 1,1 '-carbonyl-diimidazole and phenyl chloroformiate.
A particular execution of the process is that wherein R3 is methyl.
Another particular execution of the process is that wherein the appropriate ester-to-alcohol reducing agent is a metal hydride or a complex metal hydride.
In a further aspect the invention relates to a compound of formula OP Rl O N~Ra I
wherein R, Rl and RZ are as defined in claims 1 or 2 and P is an appropriate hydroxy-protecting group.
In another aspect, the invention relates to a compound of formula OP
I ~ ~CHZOH
. ~R I
wherein R is as defined in claims 1 or 2 and P is an appropriate hydroxy-protecting group.
In still another aspect the invention relates to a compound of formula OP
I ~ ~CO2R3 R
wherein R is as defined in claims 1 or 2, R3 is C1_4all~yl; and P is an appropriate hydroxy-protecting group.
Preferred are those compounds of formulae (IV), (111) or (II) wherein P is 2-(2-methoxy)propyl.
Also preferred are those compounds of formula (II) wherein R3 is methyl.
In still another aspect, the invention relates to a process for preparing a compound of formula (VI) characterized by process steps (a) and (b) as outlined above.
In still another aspect, the invention relates to a process for preparing a compound of formula (111] characterized by process step (a) as outlined above.
_g_ In still another aspect, the invention relates to a process for preparing a compound of formula (II) characterized by process steps (d) and (e) as outlined hereinafter.
The invention further provides a process preparing a compound of formula (I) characterized byprocess steps (d) and (e) as outlined hereinafter and by process steps (a), (b) and (c) as outlined above.
In a further aspect, this invention concerns the presence of polymorphic forms of the (S) - (+) - 2- (substituted phenyl) - 2- hydroxy-ethyl carbamates. In particular it concerns two polymorphic forms of the compound 2-(2-chlorophenyl)-2-(2-(2-methoxy)propyl)-ethyl carbamate The invention also concerns processes for preparing these new polymorphic forms.
Detailed Description of the Invention Subject of the present invention is a process for preparing compounds of formula (I), as outlined above, and the intermediates of formula (II), (III), (IV), and (V) as represented and defined hereinabove.
Preferred are those compounds and intermediates as defined herein wherein R is chloro, Rl and R2 are hydrogen. The compound of formula (I) wherein the substituents have the latter meanings is also referred to as 'RWJ-333369' and can be represented by the structural formula:
Cl OH
O NHZ
(I-a) The term "halogen" refers to fluoro, chloro, bromo and iodo.
"Cl_4alkyl" defines straight and branched chain saturated hydrocarbon radicals having from 1 to 4 carbon atoms such as methyl, ethyl, 1-propyl, 2-propyl, 1-butyl, 2-butyl, 2-methyl-1-propyl, 2-methyl-2-propyl. , "C1_4alkyloxy" defines C1_4alkyl radicals linked to an oxygen atom such as methoxy, ethoxy, 1-propoxy, 2-propoxy, 1-butoxy, 2-butoxy and the lilce.
"Substituted phenyl" is phenyl being substituted with the substituents outlined above.
Preferably, substituted phenyl has 1, 2 or 3 substituents. A preferred substituent is halogen, more preferably chloro.
P, as mentioned above, is an appropriate hydroxy protecting group. Preferably it should be selected such that it is stable in the reduction procedure of (In to (ffl]
as well as the subsequent reaction step from (III] to (Vn. The preferred reduction procedure being with complex hydrides as outlined hereinafter, the group P should be stable towards these complex hydrides and the reaction products therefrom. The reduction with complex hydrides requires basic conditions and hence the group P should not be cleaved in these basic conditions. The group P should preferably be removable under acidic conditions which should be such that the carbamate function is not split.
Particularly preferred are protecting groups P that are removable at a pH
which is about 1 or slightly higher.
Particularly useful are groups P of the ether type. As examples of P there may be mentioned:
methoxymethyl ethers (MOM): which can be prepared from methoxymethylchloride or formaldehyde dimethylacetal;
tetrahydropyran ethers (THP ethers) prepared from dihydropyran;
tetrahydrothioypyranyl ethers from dihydrothiopyran;
chloro substituted tetrahydrofuranyl ethers from 2-chlorotetrahydrofuran;
tetrahydrothiofuranyl ethers from dihydrothiofuran;
1-ethoxyethyl ethers from ethylvinyl ethers or 1-ethoxyethyl chloride 1-methyl-1-methoxyethyl ethers from methylvinyl ethers, which are of particular interest;
triphenyl ethers and appropriate derivatives thereof which can be prepared from the corresponding.chlorides;
benzyl ethers and appropriate derivatives thereof which can be prepared from the corresponding bromides or iodides;
4-methoxytetrahydropyranyl ethers from 5,6-dihydro-4-methoxy-2H-pyran;
4-methoxytetrahydrothiopyranyl ethers from 5,6-Dihydro-4-methoxy-2H
thiopyran.
It is furthermore advantageous to use such groups P which do not lead to a mixture of diastereomers, i.e. P groups without an asymmetric center. Under certain circumstances, e.g. depending upon the nature of the reducing agent, particular silyl ethers can be used as appropriate groups P, in particular t.butyldimethylsilyl (TBDMS), triisopropylsilyl, tribenzylsilyl, and the like.
Step (ay preparation of 2-(substituted phenyl)-2-(protected hydroxyl-ethanol (IIP
According to the first step of the process of this invention, the ester (In is reduced to the corresponding alcohol of formula (III) using an appropriate ester-to-alcohol reducing agent. The latter may be a metal hydride or a complex metal hydride such as lithium aluminium hydride or derivatives thereof.
Particular reduction agents for this reaction are silane agents such as trialkylsilanes, dialkylsilanes, trialkoxysilanes and preferably poly methylhydrogensiloxane ('PMHS') in the presence of a suitable catalyst. The latter in particular are transition metal halogenides or carboxylates, and preferably the latter is a zinc carboxylate, such as zinc hexanoate or a derivative thereof, more preferably zinc 2-ethylhexanoate, in the presence of a metal hydride such as an alkali metal or earth alkaline metal hydride, or aluminium hydride, e.g. lithium, sodium, potasium, calcium hydride, or a complex hydride such as a borohydride or aluminium hydride, in particular an alkali metal borohydride or aluminiumhydride, e.g. lithium, sodium or potassium borohydride or aluminium hydride. A combination of zinc 2-ethylhexanoate and sodium borohydride is most preferably used as the catalyst mixture. These and similar reduction agents are described in Patent Application WO 96112694 (1995) and in J. Ulinan, The Alefnbic, 1999, 59, 1 ff.
The reaction of this process step is conducted in a suitable solvent, e.g. an ether or polyether, or a hydrocarbon, in particular an aromatic hydrocarbon. Specific examples of suitable solvents comprise diethyl ether, dipropyl ether, diisopropyl ether, dibutyl ether, diglyme and toluene.
The reduction agent can be formed by stirring a mixture of the agents ERS A
and ERS
B in a separate reaction vessel (ERS = Ester Reduction System), commercially available from Rohm & Haas). ERS A is a solution of NaBH4 in tetraglyme, whereas ERS B is a solution of Zn(carboxylate)2*HZO, in particular of Zn(2-ethylhexanoate)Z
*H20, in tetraglyme. ERS A and ERS B are preferably mixed at higher temperature, e.g. at a temperature in the rage of 50 to 90°C, in particular at 70°C for a period of several minutes, e.g. for 30 min. Subsequently the ERS A and ERS B mixture is added to the ester (Ilk and ERS C is added. ERS C is poly methylhydrogensiloxane.
The reducing agent can also be generated ira situ in the reaction vessel, which is particularly attractive. In this variant, intermediate (In is dissolved in a suitable solvent, preferably in toluene at increased temperature of 80-90°C. ERS
B is added first in one portion, followed by the addition of ERS A also in one portion. Then immediately ERS C is added within one hour while controlling the temperature and keeping it at higher temperature, in particular around 95°C.
The starting mandelic acid ester (In is prepared as described hereinafter and can be isolated and optionally purified and used as such in the reduction step. The ester (Il) can also be kept dissolved in the solvent in wluch it was prepared and used as such in the reduction step.
Preferably the substituted mandelic acid ester (I~ is a methyl ester.
In a particular execution of this process step the starting ester (I~ is either used dissolved in the solvent of the previous reaction step, or it can also be solved in a suitable solvent, such as for example an ether, e.g. in di-n-butylether, or preferably in toluene. The reducing agent, prepared as above, is added in one portion to the solution, followed by the addition of ERS C within one hour. The reaction mixture optionally can be heated to 90°C prior to addition of ERS C. Then the temperature is increased to 90°C and kept at that temperature until an in-process-control shows a conversion of at least 99%. The reaction time is around 1 h. After complete reduction the mixture is cooled to 15 to 20°C and hydrolyzed carefully first with methanol and subsequently with aqueous alkali metal hydroxide solution, which preferably is a NaOH
solution in slight excess (e.g. 1.3 mol-eq., using a 30% solution).
Subsequently, the mixture is refluxed for about 1 h at about 50°C and the layers are separated at room temperature. The organic layer is washed with water and with saturated aqueous NaCI at room temperature.
The quantity of ERS C is in the range of 2 to 4, in particular in the range of 2.2 to 3 molar equivalents, preferably 2.3 molar equivalents of ERS C are used.
The reaction typically is complete after about 1 hour.
After completion of the reduction reaction, the excess of ERS C can be destroyed with a suitable ester, in particular with ethyl acetate. After addition of the said ester, the mixture is stirred for one hour and hydrolyzed at 90°C by addition of aqueous base solution, preferably a NaOH or a KOH-solution (e.g. of 33%) and further preferably with the use of methanol. Further work-up comprises the separation of the organic layer and washing with aqueous basic solution (e.g. I~OH-solution of 33%) and with water.
The resulting methylester is an oil, and, if desired, can be distilled for purification.
Step (b)' preparation of 2-(substituted phenyl)-2-(protected hydroxyl-ethyl carbamate (VP
W this step the alcohol of formula (~ is reacted with a carbonyl compound of formula O
X ~Y
wherein X and Y are appropriate leaving groups. Preferably one of X or Y is more reactive than the other. X and Y can be halogen, in particular chloro or bromo, but preferably X and Y are imidazolyl groups. If X is halo, Y preferably is an aryloxy or alkoxy group. In the latter instance (V) is an alkyl or aryl halo formiate.
Particular aryl groups in (TV) are phenyl or substituted phenyl, e.g. halophenyl, or C1_4 alkyl. A
preferred example of (IV) is phenyl chloroformiate or l, l '-carbonyl-diimidazole.
The reaction is conducted in a suitable solvent such as a hydrocarbon, in particular an aromatic hydrocarbon, e.g. toluene, or in an ether, e.g. THF. The reaction temperature depends upon the reactivity of the reagent (IV) but in general is room temperature or lower. In case N,N'-carbonyl diimidazole is used as reagent the reaction preferably is conducted at room temperature (i.e.. at about 25 °C).
The reaction typically is complete after less than 1 hour, e.g. after about %2 hour. The reaction product of this reaction is usually not isolated; it can be represented by the following formula:
OP
O Y
R
O
(~-a) wherein Y is as defined hereinabove and in particular is an imidazolyl group, or an aryloxygroup, e.g. a phenoxy or substituted phenoxy group. The intermediates of formula (IV-a) are deemed novel and constitute an additional feature of the present invention. Preferred intermediates of formula (IV-a) are those wherein Y is imidazol-1-yl.
The product of he previous reaction, i.e. the intermediate of formula (IV-a), is usually not isolated and is reacted immediately with the amine of formula (V) as specified above. A preferred amine is ammonia, but it can also be an ammonium salt. In that instance the ammonia or an ammonium salt is in an aqueous medium and added to the solution of intermediate (IV-a) at room temperature.
Vigorous stirring is recommended when using (V) in aqueous media, because of the two phase system. The reaction is terminated after several hours, in particular after about 4 hrs. The organic phase is separated and the product can optionally be isolated and purified. The organic phase with product (VI) dissolved therein can also be used as such in the subsequent reaction step.
Ste~c~ preparation of 2-(substituted phenyl)-2-hydroxyethyl carbamate (I) This reaction step involves the deprotection of the hydroxy function and depends on the nature of the group P.
Where P is 2-methoxy-2-propyl, removal is by addition of an appropriate acid, e.g.
hydrochloric acid.
In a preferred execution, product (VI) is used dissolved in the solvent of the previous step. Water and concentrated hydrochloric acid are added while stirnng.
Already after a few minutes the reaction is almost completed and the end procuct (I) starts precipitating. The reaction mixture is stirred for a couple of hours, in particular for about 4 hours because in this Way the end product can be filtered better.
Subsequently the end product is filtered off and washed.
The end product (I) can be recrystallized from a suitable solvent such as an alcohol, e.g.
methanol, preferably with addition of acidified water.
Starting materials The starting materials(I~ are obtained by a process which is characterized by:
(d) an esterification reaction of an appropriately substituted mandelic acid of formula:
OH
I ~ ~COOH
R
(V
thus preparing the corresponding ester of formula OH
~COOR3 R
(~) wherein in (VIII) and (IX) R and R3 are as defined above and R preferably is 2-chloro and/or R3 preferably is methyl; and (e) treating the ester (IX) with a suitable reagent generating a hydroxy protecting group, thus preparing an intermediate of formula OP
~COOR3 R
i (~
wherein R and P are as defined above.
The ester (IX) is reacted with an appropriate agent capable of introducing a hydroxy protecting group. A preferred agent is 2-methoxypropene.
Alternatively, the sequence of the above steps may be switched, i.e. the hydroxy protecting group may be introduced and subsequently the ester formed.
Step (d): Preparation of substituted mandelic acid esters (IX) According to this reaction step the starting acid (V~ is reacted in the alcohol of which IS the ester (IX) is derived. Typically a C1_4 alkanol is used, preferably methanol, thus yielding the corresponding C1_4 alkyl esters or preferably the methyl ester of (VITI).
The reaction is conducted with an excess of a strong acid, preferably a hydrohalic acid such as HCl, in particular with 1-4 molar equivalents, preferably with 2.5 molar equivalents of concentrated HCI. The reaction also works with a catalytic amount of sulfuric acid or also with SOCl2 . In the latter instance the reaction is highly exothermic, requiring appropriate measures for controlling the temperature.
The reaction preferably is conducted at room temperature or slightly increased temperatures, preferably not higher than about 30°C. The reaction time usually is less than about 1 hour, e.g. about 30 min. The resulting ester (IX) typically is an oily compound which is used as such in the subsequent process steps. In a preferred execution, the ester (IX) is kept in the solvent in which it was made and is used further dissolved in this solvent.
Step (ey Preparation of h~~protected substituted mandelic acid esters (ll~.
The reaction conditions of this step depend on the nature of protecting group P.
_ In a preferred execution, P is 2-methoxy-1-propyl which is derived from 2-methoxypropene. The latter is dissolved in a suitable solvent, in particular the solvent in which the other reaction steps are conducted. This solution is added to a solution of intermediate (IX) in a suitable solvent which has been acidified, e.g. by addition of hydrochloric acid, in particular by adding gaseous hydrochloric acid over the solution. The pH should preferably be low, e.g. pH 1-2. The solvent of intermediate (IX) should preferably be the same as that wherein the 2-methoxypropene is dissolved and more preferably should be the same as the solvent used in the other reaction steps.
The reaction is complete in less than 1 hour, normally witlun half an hour.
The process according to the present invention yields the end product (n in high yield and purity and can be scaled up to production size batches. A particular aspect of the current process is that it leaves the stereochemical integrity intact of the asymmetric center on the carbon atom bearing the hydroxy function, i.e. the present process shows neglectable or no racemisation.
The various intermediate products of the process, including the steps for preparing the starting materials, can be isolated and if desired further purified before further use in a next step. Alternatively, all the process steps, if desired also including the steps for preparing the starting materials, can be conducted in the same solvent, i.e.
without isolation and optional purification of the intermediate products. In the latter instance it may be advantageous to distil off some of the solvent or to add some of it during one or more of the reaction steps. A suitable solvent for the one solvent execution of the process is an aromatic hydrocarbon, preferably toluene. It is also possible to conduct a certain number of steps in one solvent and the others in another.
Conducting the whole process in one solvent has the particular advantage that the process is much simpler and can be conducted more quickly without having to discard or recuperate solvents, which is advantageous economically as well as from an enviromnental aspect.
_ Pol,>~rphs The present invention is further directed to novel crystalline structures of the compound of formula (I) wherein R is 2-chloro, Rl and R2 are hydrogen, said compound hereinafter being referred to as compound (I-a).
The crystalline forms of compound (I-a) may be prepared by an appropriate recrystallization of compound formula (I-a) from a suitable organic solvent.
Depending upon the recrystallisation procedure either form A or form B can be obtained.
One crystalline form of compound (I-a) is referred to as 'form A' and is prepared by recrystallisation of compound (I-a) from a suitable solvent. The temperature in this recrystallisation procedure is kept below 60 °C, in particular below 50 °C. Suitable solvents are those wherein the compound of formula (I-a) dissolves at higher temperature and is relatively poorly soluble at lower temperature, e.g. at a temperature lower than 20 °C, or lower than 10 °C, or even lower than 0 °C, or -10 °C. Suitable solvents are the lower alkanols, i.e. the C1_4alkanols and in particular methanol.
In one type of embodiment, the compound (I-a) is dissolved by heating or refluxing in methanol, or by heating in a lower alkanol. The temperature of the mixture should not allowed to exceed 60 °C. Subsequently, the solution is cooled, preferably slowly, e.g.
by simply allowing the solution to cool. At a temperature of about 50 °C crystallization already starts. The mixture is stirred at room temperature for 15-20 hours whereupon acidified water is added. The water preferably is acidified with a strong acid, e.g.
hydrochoric acid or a similar acid to a pH value of about 3 to 4, in particular about pH
3.5. The mixture is further cooled to about 0 to 10 °C, in particular to about 5 °C and stirred at that temperature for a sustained period of time, e.g. about 1 hour.
The crystalline end product is then filtered and dried.
In a further aspect the present invention concerns the compound (I-a) predominantly in Form A. The invention in particular concerns compound (I-a) occurring as a polymorph mixture, which predominantly contains Form A. More in particular the invention concerns compound (I-a), occurring as polymorph mixture containing at least 90 % or _ more of form A, further in particular 95 % or more of Form A, still further in particular 99 % or more of Form A.
Hence, recrystallization of the compound of formula (I-a) as described above yields a novel crystalline form of (I-a), herein referred to as 'Form A'.
Compound (I-a) in Form A has a particular crystalline form, i.e. the monoclinic crystalline form.
One crystalline form of compound (I-a) is referred to as 'form B' and is prepared by recrystallisation of compound (I-a) from a suitable solvent. The temperature in this recrystallisation procedure is brought above 60 °C, in particular above 70 °C. Suitable solvents are those wherein the compound of formula (I-a) dissolves at higher temperature and is relatively poorly soluble at lower temperature, e.g. at a temperature lower than 20 °C, or lower than 10 °C, or even lower than 0 °C, or -10 °C. Suitable solvents are the lower alkanols, e.g. the C3_4alkanols and in particular propanol (n-propanol or 2-propanol). Other suitable solvents are esters such as ethyl acetate or a similar solvent, or mixtures thereof with lower boiling halogenated hydrocarbons such as trichloromethane or dichloromethane, which is preferred. In this instance, preferably, the starting material is first dissolved in the ethyl acetate after which the halogenated hydrocarbon is added. The volume of halogenated hydrocarbon that is used is equal to about five times (v/v) relative to the volume of ethyl acetate, preferably the volume ratio is in the range of about 1 : 2 to about 1: 5, e.g. it can be about 1 : 3 (ethylacetate halogenated hydrocarbon). Still further suitable solvents are polyols, in particular the glycols such as ethylene glycol, which is preferred, or propylene glycol, butylene glycol and the like. Water can be added, in particular where polyols are used as a solvent. If water is added, it may be acidified with a suitable strong acid such as hydrochloric acid to low pH, e.g. a pH which is in the range of pH 2 - 5, e.g. a pH which is about pH 3.
Water can be added in various quantities. For example where ethylene glycol or similar glycols are used, the volume ratios of glycol to added water are in the range of 1 : 1 to about 1 : 8, or 1 : 2 to 1 : 5, e.g. about 1 : 4 (glycol : water, v/v).
In one type of embodiment, the compound (I-a) is dissolved by heating or refluxing in 2-propanol, ethyl acetate or a mixture of ethylacetate/dicloromethane, more preferably a 1: 3 mixture of ethylacetate/dichloromethane. Subsequently the solution is allowed to cool whereupon the desired product crystallizes.
This procedure can also be used to convert form A into form B, i.e. by replacing the compound (I-a) by form A in the above procedure.
Form B can also obtained in a highly pure form by heating form A to 130°C over a period of 60 min (DSC experiment) as triclinic crystals.
In a further aspect the present invention concerns the compound (I-a) predominantly in Form B. The invention in particular concerns compound (I-a) occurring as a polymorph mixture, which predominantly contains Form B. More in particular the invention concerns compound (I-a) occurring as polymorph mixture containing at least 90 % or more of form B, further in particular 95 % or more of Form B, still further in particular 99 % or more of form B.
The novel crystalline forms of the compound of formula (I-a) may be characterized by their respective X-ray powder diffraction patterns utilizing appropriate powder diffractometers, in particular using the methodology as outlined in the Examples.
In a further aspect, this invention provides a process for preparing form A of the compound of formula (I-a), or the compound of formula (I-a) predominantly in form A, said process comprising dissolving the compound of formula (I-a) in a suitable solvent, heating the solvent to a temperature which is lower than about 60 °C
and higher than about 50 °C, and subsequently allowing to cool said solution. Suitable solvents are alcohols, in particular C1_~ alkanols, preferably methanol. In a particular execution of this process, the heated solution is allowed to cool until the first crystals appear, in particular the solution is allowed to cool to about 50 °C allowing the appearance of the first crystals, and subsequently allowed to cool further, in particular to room temperature.
In another aspect, this invention provides a process for preparing form B of the compound of formula (I-a), or the compound of formula (I-a) predominantly in form B, said process comprising recrystallisation of compound (I-a) from a suitable solvent at a temperature of 60 °C or higher, in particular of 70 °C or higher. Suitable solvents are, for example, the lower alkanols, e.g. the C3_4alkanols and in particular propanol. Other suitable solvents are ethyl acetate or mixtures thereof with lower boiling halogenated hydrocarbons such as dichloromethane.
The following Examples describe the invention in greater detail and are intended to illustrate the invention, but not to limit it.
Examples Preparation of (~-(+)-2-(2-chlorophenyl)-2-hydroxy-ethyl carbamate (compound (I-a)) Example 1 (,.5~-(+)-2-Chloromandelic acid methyl ester (Intermediate 1) (,$~-(+)-2-Chloromandelic acid (100.0 g, 535.9 mrnol) is dissolved at rt in methanol (553.0 g). After cooling to 10 ~ 5°C, hydrogen chloride gas (55.3 g) is conducted over the solution for 30 min holding the temperature below 25 ~ 5°C. The course of this reaction and the following reactions is followed by HPLC. Trimethyl orthoformate (62.6 g, 589.5 mmol) is added at 20~5°C to the colorless to light yellow solution which is stirred for 30 min at the same temperature. Thereafter the solvent and the hydrogen chloride gas is removed as far as possible irz vacuo (40 ~ 5°C, 40 ~ 10 mbar). The oily residue is diluted with toluene (130 g) and the solvent is removed again as far as possible in vacuo. Toluene (261 g) is added and the solution is cooled to 15 ~
5°C.
Example 2 2-Methoxy-1-proRyl derivatized (~-(+)-2-Chloromandelic acid methyl ester (Intermediate 2) Hydrogen chloride gas (0.55 g, 15 mmol) is conducted over the solution (pH-value drops from 3 to 1-2). In a second flash, 2-methoxy-propene (78.0 g, 1081.7 mmol) is dissolved in toluene (120 g) at 20 ~ 5°C and the above prepared solution of Intermediate 1 is added at a temperature range of 25~5°C (ca. 30 min).
After the addition is complete, the mixture is stirred for 30 min. Triethylamine (14.0 g, 138.3 mmol) is added to the colorless to light yellow solution, it is stirred at rt for 5 min and diluted with toluene (402 g) (pH >_ 8, if not, addition of triethylamine). The mixture is washed with water (1 x 150 g), aq. sodium hydrogencarbonate solution (5%, 1 x g), and aq. sat. sodium chloride solution (1 x 150 g). Drying with sodium sulfate (ca. 65 g), filtration, and removal of ca. 86 g toluene ih vacuo leads to Intermediate 2.
Example 3 2-(2-Chloro~henyl)-2-~2-(2-methoxy)propyl)-ethanol (Intermediate 3) At first VenpureTM ERS B (13.0 g) and secondly VenpureTM ERS A (13.0 g) is added and the mixture is heated within 45 min to 85~5°C. The appearance of the solution turns from clear to slightly cloudy. VenpureTM ERS C (73.9 g, ca. 1239.4 mmol) is dropped into the solution in such a way that the temperature is 95 ~5° C (ca. 45 min, delay of the start of the exothermic reaction is possible). The reaction is finished 15 min after the end of the dropping which is also indicated by an additional milky to gray (from zinc) appearance in the mixture. If not, an additional 7.0 g of each VenpureTM ERS B and VenpureTM ERS A are added directly to the reaction mixture and the whole is heated until the conversion is complete. The solution is cooled to 15 ~ 5°C and methanol (30 g) is added (hydrogen evolution). Aqueous sodium hydroxide solution (30%, 238.0 g) is added dropwise while holding the temperature below 20°C (ca. 30 min, above 25°C, a violent foaming is observed). After the addition is finished the two phase mixture is heated for 1 h to 50 ~
5°C, and the previously formed precipitate dissolves now. The phases are separated after cooling to-rt and the colorless organic phase is washed with water (1 x 200 g) and with aq. sat.
sodium chloride solution (1 x 200 g). Drying with sodium sulfate (ca. 65 g), filtration, and removal of ca. 180 g solvent in. vacuo gives a solution of Intermediate 3.
Example 4 2-(2-chlorophenyl)-2-(2-(2-methoxy)propyll-ethyl carbamate (Intermediate 5) To the solution obtained in example 3, a slurry of 1,1 '-carbonyl-diimidazole (103.8 g, 641.4 mmol) in toluene (180 g) is added within 30 min. at a temperature in the range of 25~5°C. The conversion to 1-imodazolyl-1' - [2- (2-chlorophenyl) -2 -[2- (2-methoxypropyl]- ethoxy carbonyl (Intermediate 4) is then complete.
Toluene (200 g) and aq. ammonium hydroxide solution (25%, 364 g) are added.
After 3 h vigorous stirring at rt, the phases are separated and the organic phase containing Intermediate 5 is washed with water (1 x 200 g) and with aqueous saturated sodium chloride solution (1 x 200 g).
Example 5 Preparation of Compound (I-a) To the organic phase containing Intermediate 5, prepared as described above, is added water (160 g) and conc. aq. hydrochloric acid (39 g) generating a pH-value <1Ø
Compound (I-a) starts precipitating while stirring after 5 min at rt. After 4 h, the product is filtered off, the filter cake is washed with water (3 x 75 g) and with toluene (3 x 44 g). 96.9 g compound (I-a) (purity 99.8%, assay 99.0% determined by HPLC, ee >99.9% determined by chiral HPLC , 444.8 mmol, overall yield 83.0%) after drying (50~5°C, 40~10 mbar).
Example 6 Preparation of Form A of Compound (I-a) This material of the previous example is suspended in methanol (115 g) and after heating to reflux, the formed solution is hot filtered, cooled to rt, and stirred for 15-20 h at this temperature. Water (577 g) containing aq. cone. hydrochloride acid (ca. 13 mg, pH-value of the solution is 3.70.2) is added. The mixture is cooled to 5~5°C, stirred for 2 h at the same temperature, and then filtered. The filter cake is washed with water (3x 30 g). After drying (50~5°C, 50~10 mbar), 93.0 g of Form A of comRound (I-a) (purity 100%, assay 99.7%, ee >99.9%, 430.0 mmol, overall yield 80.2%) is obtained as colorless needles.
Example 7 Determination of pol~nnorphic form b~powder X-ray diffractometry Sample preparation About 0.5 to 1 g of sample is gently pressed into a powder sample holder in order to get a well defined, smooth surface.
Instrument A computer controlled powder diffractometer system APD1700 (Philips) with an automated divergence slit and secondary monochromator or equivalent equipment is used.
Recording conditions Copper radiation: Kal = 0.15406 and K~ = 0.15444 nm Voltage: 40 kV
Current: 30 mA
Divergence slit: automated Receiving slit: 0.1 °
Graphite secondary monochromator for Cu-I~°,1 Xe proportional counter Counting starts at 1.5° 20 and proceeds in steps of 0.02° 20 to reach 40° 20. The counting time per interval is 3 sec and the total recording time is 2 h 50 min.
Form A of the compound of formula (I-a) may be characterized by its X-ray diffraction pattern, which comprises the major pealcs as listed in the Table 1 in the Examples.
TABLE 1. FORM A POWDER X-RAY DIFFRACTION PEAKS
Form B of the compound of formula (11) may be characterized by its X-ray diffraction pattern, which comprises the major peaks as listed in Table 2.
Form A
Angle d value Intensity 2-Theta Angstrom Cps 9.217 9.58681 4610 100.0 10.506 8.41395 108 2.3 14.954 5.91952 986 21.4 17.375 5.09990 1501 32.6 18.435 4.80892 3287 71.3 20.028 4.42979 884 19.2 20.720 4.28343 286 6.2 21.045 4.21801 2535 55.0 22.205 4.00026 80.1 1.7 23.257 3.82165 1248 27.1 24.954 3.56544 494 10.7 25.715 3.46166 1776 38.5 26.093 3.41233 684 14.8 27.379 3.25489 3953 85.8 27.689 3.21908 954 20.7 29.339 3.04172 163 3.5 30.134 2.96333 517 11.2 31.480 2.83961 129 2.8 31.780 2.81347 310 6.7 32.139 2.78287 113 2.4 32.880 2.72180 318 6.9 33.097 2.70446 337 7.3 34.664 2.58570 479 10.4 35.170 2.54967 972 21.1 35.500 2.52667 464 10.1 35.995 2.49305 109 2.4 36.700 2.44679 250 5.4 36.958 2.43029 374 8.1 37.314 2.40791 1034 22.4 38.349 2.34527 408 8.9 39.222 2.29508 161 3.5 39.683 2.26945 310 6.7 Example 8 Preparation of Form B of Compound (I-al 5.0 g (19.0 mmol) raw RWJ-333369 (polymorph A) is dissolved in 4.75 g 2-propanol by heating to reflux. This solution is cooled to room temperature within 30 min whereby the substance crystallizes. After additional stirring at 4°C
for 1 h, the product is filtered off and dried at 80°C and 20 mbar for 8h. Yield: 4.0 g (15.2 mmol, 80%) polymorphic form B.
2-Theta d-value Intens. Rel.Int.
9.13 9.686 486.0 0.324 10.38 8.522 198.0 0.132 12.81 6.910 334.0 0.223 15.04 5.890 507.0 0.338 15.92 5.567 153.0 0.102 17.32 5.120 594.0 0.396 18.31 4.845 694.0 0.463 18.58 4.775 282.0 0.188 19.37 4.582 239.0 0.159 20.04 4.431 326.0 0.217 20.81 4.268 864.0 0.576 21.72 4.092 324.0 0.216 22.15 4.013 1500.0 1.000 23.25 3.826 661.0 0.441 24.94 3.570 416.0 0.277 25.64 3.474 516.0 0.344 27.20 3.278 1044.0 0.696 27.59 3.233 506.0 0.337 28.23 3.161 216.0 0.144 28.56 3.125 221.0 0.147 29.44 3.034 208.0 0.139 30.34 2.946 328.0 0.219 30.83 2.900 314.0 0.209 31.77 2.816 259.0 0.173 32.13 2.786 200.0 0.133 32.68 2.740 335.0 0.223 33.04 2.711 276.0 0.184 _28_ 34.30 2.614 207.0 0.138 34.81 2.577 621.0 0.414 35.29 2.543 244.0 0.163 35.91 2.501 243.0 0.162 36.36 2.471 189.0 0.126 37.08 2.424 412.0 0.275 37.66 2.388 349.0 0.233 38.55 2.335 431.0 0.287 39.09 2.304 321.0 0.214
Claims (14)
1. A process for preparing a compound of formula wherein: R is halogen; R1 and R2 independently are hydrogen or C1-4alkyl, optionally substituted with phenyl or substituted phenyl, wherein substituted phenyl has substituents selected from halogen, C1-4alkyl, C1-4alkyloxy, amino, nitro and cyano;
said process comprising (a) reducing an ester of formula:
wherein P is an appropriate alcohol-protecting group; R3 is C1-4alkyl; with an appropriate ester-to-alcohol reducing agent, thus obtaining an alcohol of formula:
(b) reacting the alcohol of formula (III) with a carbonyl compound of formula wherein X and Y are appropriate leaving groups; and subsequently with an amine of formula thus obtaining a compound of formula:
; and (c) removing the protecting group P thus obtaining a compound of formula (I).
said process comprising (a) reducing an ester of formula:
wherein P is an appropriate alcohol-protecting group; R3 is C1-4alkyl; with an appropriate ester-to-alcohol reducing agent, thus obtaining an alcohol of formula:
(b) reacting the alcohol of formula (III) with a carbonyl compound of formula wherein X and Y are appropriate leaving groups; and subsequently with an amine of formula thus obtaining a compound of formula:
; and (c) removing the protecting group P thus obtaining a compound of formula (I).
2. A process according to claim 1, wherein R is 2-chloro, R1 and R2 are hydrogen.
3. A process according to claim 1 or 2, wherein the alcohol protecting group is selected from 2-(2-methoxy)propyl.
4. A process according to claim 1 or 2, wherein the carbonyl compound of formula (IV) is selected from diimidazolyl carbonyl, aryl or substituted aryl haloformate.
5. A process according to claim 1 or 2, wherein R3 is methyl.
6. A process according to claim 1 or 2, wherein the appropriate ester-to-alcohol reducing agent is a metal hydride or a complex metal hydride.
7. A process according to any one of claims 1 to 6, wherein said ester of formula (II) is prepared by (i) esterifying a substituted mandelic acid of formula (VIII) to obtain a corresponding ester of formula (IX) wherein R and R3 are as defined in any one of claims 1 to 6; (ii) treating the ester of formula (IX) with a suitable reagent generating a hydroxy protecting group, thus preparing the ester of formula (II).
8. The process of claim 7, wherein R is 2-chloro.
9. The process according to claim 7 or 8, wherein the esterification is performed in the presence of a C1-C4 alcohol.
10. The process according to any one of claims 7 to 9, wherein R3 is methyl.
11. The process according to any one of claims 7 to 10, wherein said reagent is 2-methoxypropane.
12. The process according to any one of claims 7 to 11, wherein esterification is conducted after generating the hydroxyl protecting group -OP.
13. A compound of formula wherein R, R1 R2and P are as defined in any one of claims 1 to 12.
14. A compound according to claim 13, wherein the group -OP is selected from the group consisting of methoxymethyl ethers; tetrahydropyran ethers;
tetrahydrothiopyran ethers; chloro substituted tetrahydrofuranyl ethers; tetrahydrothiofuranyl ethers; 1-ethoxyethyl ethers; 1-methyl-l-methoxyethyl ethers; triphenyl ethers; benzyl ethers; 4-methoxytetrahydropyranyl ethers; and 4-methoxytetrahydrothiopyranyl ethers.
tetrahydrothiopyran ethers; chloro substituted tetrahydrofuranyl ethers; tetrahydrothiofuranyl ethers; 1-ethoxyethyl ethers; 1-methyl-l-methoxyethyl ethers; triphenyl ethers; benzyl ethers; 4-methoxytetrahydropyranyl ethers; and 4-methoxytetrahydrothiopyranyl ethers.
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CZ (1) | CZ2004718A3 (en) |
EE (1) | EE05381B1 (en) |
HR (1) | HRP20040557A2 (en) |
HU (1) | HUP0402491A2 (en) |
IL (3) | IL162405A0 (en) |
MX (1) | MXPA04006135A (en) |
MY (1) | MY142415A (en) |
NO (1) | NO20043105L (en) |
NZ (1) | NZ533592A (en) |
PL (1) | PL370977A1 (en) |
SK (1) | SK2572004A3 (en) |
TW (1) | TWI333944B (en) |
WO (1) | WO2003053916A1 (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
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US7767843B2 (en) * | 2006-03-02 | 2010-08-03 | Apotex Pharmachem Inc. | Process for the preparation of phenylcarbamates |
BRPI0718131A2 (en) * | 2006-10-06 | 2013-11-05 | Transform Pharmaceuticals Inc | (S) - (+) - 2- (2-Chlorophenyl) -HYDROXY-ETHYL CARBAMATE CRYSTAL |
US20090105498A1 (en) * | 2007-10-18 | 2009-04-23 | Porstmann Frank | Improved process for preparing 2-(substituted phenyol)-2-hydroxy-ethyl-carbamates |
US8609849B1 (en) | 2010-11-30 | 2013-12-17 | Fox Chase Chemical Diversity Center, Inc. | Hydroxylated sulfamides exhibiting neuroprotective action and their method of use |
KR101862203B1 (en) * | 2011-12-27 | 2018-05-29 | (주)바이오팜솔루션즈 | Phenyl alkyl carbamate derivative compound and pharmaceutical composition containing the same |
KR102421006B1 (en) * | 2016-05-19 | 2022-07-14 | 에스케이바이오팜 주식회사 | Use of carbamate compound for prophylactic treatment of headache |
Family Cites Families (6)
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FR5671M (en) * | 1965-04-23 | 1968-01-02 | ||
US5504108A (en) * | 1990-01-12 | 1996-04-02 | The Ohio State University Research Foundation | Optically pure 4-aryl-2-hydroxytetronic acids |
JP3010497B2 (en) * | 1990-05-31 | 2000-02-21 | チッソ株式会社 | Method for producing optically active α-hydroxyesters |
CN1091087C (en) | 1994-10-19 | 2002-09-18 | 弗门尼舍有限公司 | Method for preparing alcohols |
US5698588A (en) | 1996-01-16 | 1997-12-16 | Yukong Limited | Halogen substituted carbamate compounds from 2-phenyl-1,2-ethanediol |
WO2001040168A1 (en) * | 1999-11-29 | 2001-06-07 | Mitsubishi Rayon Co., Ltd. | Acetalsulfonate derivative, process for producing the same, and process for producing styrene oxide derivative |
-
2002
- 2002-12-19 CN CNB028281128A patent/CN100457723C/en not_active Expired - Lifetime
- 2002-12-19 EP EP20100174144 patent/EP2248799B1/en not_active Expired - Lifetime
- 2002-12-19 KR KR1020097016975A patent/KR20090097966A/en active Application Filing
- 2002-12-19 BR BR0215237-1A patent/BR0215237A/en not_active Application Discontinuation
- 2002-12-19 EP EP02793127A patent/EP1461309A1/en not_active Ceased
- 2002-12-19 SK SK257-2004A patent/SK2572004A3/en unknown
- 2002-12-19 CZ CZ2004718A patent/CZ2004718A3/en unknown
- 2002-12-19 AU AU2002358806A patent/AU2002358806B2/en not_active Expired
- 2002-12-19 MX MXPA04006135A patent/MXPA04006135A/en active IP Right Grant
- 2002-12-19 JP JP2003554633A patent/JP4610899B2/en not_active Expired - Lifetime
- 2002-12-19 PL PL02370977A patent/PL370977A1/en not_active Application Discontinuation
- 2002-12-19 HU HU0402491A patent/HUP0402491A2/en unknown
- 2002-12-19 WO PCT/EP2002/014843 patent/WO2003053916A1/en active Application Filing
- 2002-12-19 IL IL16240502A patent/IL162405A0/en unknown
- 2002-12-19 NZ NZ533592A patent/NZ533592A/en not_active IP Right Cessation
- 2002-12-19 EE EEP200400098A patent/EE05381B1/en not_active IP Right Cessation
- 2002-12-19 CA CA2471485A patent/CA2471485C/en not_active Expired - Lifetime
- 2002-12-19 CA CA002681964A patent/CA2681964A1/en not_active Abandoned
- 2002-12-20 TW TW091137385A patent/TWI333944B/en not_active IP Right Cessation
- 2002-12-20 MY MYPI20024814A patent/MY142415A/en unknown
- 2002-12-23 AR ARP020105084A patent/AR038055A1/en unknown
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2004
- 2004-06-08 IL IL162405A patent/IL162405A/en active IP Right Grant
- 2004-06-11 BG BG108759A patent/BG108759A/en active Pending
- 2004-06-16 HR HR20040557A patent/HRP20040557A2/en not_active Application Discontinuation
- 2004-07-20 NO NO20043105A patent/NO20043105L/en not_active Application Discontinuation
-
2009
- 2009-09-04 AU AU2009212987A patent/AU2009212987A1/en not_active Withdrawn
-
2011
- 2011-04-08 AU AU2011201613A patent/AU2011201613A1/en not_active Abandoned
- 2011-07-06 IL IL213960A patent/IL213960A0/en unknown
Also Published As
Publication number | Publication date |
---|---|
MXPA04006135A (en) | 2004-11-01 |
BR0215237A (en) | 2004-11-16 |
AU2011201613A1 (en) | 2011-04-28 |
EP2248799A1 (en) | 2010-11-10 |
BG108759A (en) | 2005-03-31 |
IL213960A0 (en) | 2011-08-31 |
TWI333944B (en) | 2010-12-01 |
NO20043105L (en) | 2004-07-20 |
CN1620425A (en) | 2005-05-25 |
SK2572004A3 (en) | 2005-02-04 |
HUP0402491A2 (en) | 2005-04-28 |
IL162405A (en) | 2011-08-31 |
AU2002358806A1 (en) | 2003-07-09 |
JP2005513126A (en) | 2005-05-12 |
WO2003053916A1 (en) | 2003-07-03 |
CZ2004718A3 (en) | 2004-12-15 |
CA2681964A1 (en) | 2003-07-03 |
EP1461309A1 (en) | 2004-09-29 |
EP2248799B1 (en) | 2015-05-20 |
IL162405A0 (en) | 2005-11-20 |
PL370977A1 (en) | 2005-06-13 |
CA2471485A1 (en) | 2003-07-03 |
HRP20040557A2 (en) | 2005-04-30 |
AU2002358806B2 (en) | 2009-09-10 |
TW200405809A (en) | 2004-04-16 |
EE200400098A (en) | 2004-10-15 |
MY142415A (en) | 2010-11-30 |
EE05381B1 (en) | 2011-02-15 |
KR20090097966A (en) | 2009-09-16 |
NZ533592A (en) | 2006-05-26 |
CN100457723C (en) | 2009-02-04 |
JP4610899B2 (en) | 2011-01-12 |
AU2009212987A1 (en) | 2009-10-01 |
AR038055A1 (en) | 2004-12-22 |
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